Division of Plastic and Reconstructive Surgery Resources
In this video you’ll join the Delaney family on their journey, learn about the large team involved in the separation surgery, and see how Abby and Erin are doing today.
In this video, clinicians and patient families talk about the diagnosis and treatment of cleft lip and palate, the most common congenital facial anomaly.
In this video, clinicians and patient families talk about the diagnosis and treatment of craniofacial conditions, including craniosynostosis, hemifacial microsomia, and other syndromes.
CHOP brings specialty and surgical services to families in our Specialty Care and Ambulatory Surgery Centers. The centers allow families access to the services of renowned Children's Hospital surgeons without a trip to the city.
An update on Abby and Erin Delaney, who were born conjoined and separated at Children's Hospital of Philadelphia (CHOP). Now now 2½ years old, they are making amazing strides in their growth and development.
AdoptCleft is a support group for parents wanting to adopt cleft children, parents that have cleft children (biological or adopted), and others that can contribute or learn from the conversations.
ACPA is an international nonprofit medical society of healthcare professionals who treat and/or perform research on birth defects of the head and face.
The American Society of Plastic Surgeons (ASPS) offers information about cleft lip and cleft palate repairs.
Changing Faces us a charity that helps improve the lives of people with craniofacial abnormalities and transform public attitudes toward people with an unusual appearance.
This foundation provides support to individuals with CHARGE syndrome and their families.
The Children's Craniofacial Association empowers and gives hope to individuals and families affected by facial differences.
The Cleft Advocate educates and inspires families whose lives are touched by cleft lip and/or palate or other craniofacial anomalies.
CPF is a nonprofit organization that enhances the quality of life for individuals affected by cleft lip and palate and other craniofacial birth defects.
FACES: The National Craniofacial Association assists children and adults who have craniofacial disorders resulting from disease, accident or birth.
March of Dimes is an international organization that works to prevent birth defects, premature birth, and infant mortality and to support expectant and new parents.
Philly Phaces provides peer support, advocacy, and resources to help Philadelphia-area children facing appearance differences from craniofacial abnormalities and cleft lip and palate.